usmle review series in pharmacology · 2012-09-22 · general principles in pharmacology objectives...

USMLE REVIEW SERIES IN PHARMACOLOGY

Henry M. Zeidan, Ph.D; FACB

Professor of Biomedical Sciences

www.ZMedicalEducation.com

Dr. Henry Zeidan 1

Dr. Henry Zeidan 2

General Pharmacologic Principles

Henry M. Zeidan, Ph.D; FACB

Professor of Biomedical Sciences

Albert Einstein

• Life is like riding a bicycle. To keep your balance, you must keep

moving.

In Santa Barbra, 1933 3 Dr. Henry Zeidan

Biomedical Sciences “A CHESS GAME APPROACH”

www.ZEdcationcenter.com

4 Dr. Henry Zeidan

http://www.zedcationcenter.com/

General Principles In Pharmacology Objectives

State in words what is meant by the terms, Pharmacology, Pharmacodynamics Pharmacokinetics, Pharmaceutics,

Pharmacotherapeutics and Pharmacognosy

Define the term pKa both mathematically and in words. Write the Henderson-Hasselbalch equation.

5 Dr. Henry Zeidan

Objectives(Cont’d) •

Demonstrate how the Henderson-Hasselbalch equation

shows how the state of ionization of a group on a molecule will vary with pH.

Distinguish the term pharmacokinetics from pharmacodynamics.

Identify the processes comprising the acronym ADME and classify those processes as relating to pharmacokinetics pharmacodynamics.

6 Dr. Henry Zeidan

General Principles In Pharmacology Objectives(Cont’d) • D •

State the overall objective of drug biotransformation.

Identify the primary location of drug biotransformation and define the term first pass effect.

Describe the role of cytochrome P450 enzymes in drug biotransformation.

Explain enzyme induction and enzyme inhibition and how these processes may affect plasma levels of a drug.

Explain how biotransformation can lead to toxic and active metabolites.

7 Dr. Henry Zeidan

Objectives(Cont’d)

Distinguish between Phase I and Phase II biotransformation reactions.

Identify the various types of Phase I biotransformation reactions and their common purpose. Identify the molecules or groups involved in Phase II biotransformation reactions.

8 Dr. Henry Zeidan

General Principles In Pharmacology Objectives

• 5

Define the term ‘prodrug’ and give examples of prodrug use to meet different goals. Explain the differing effects of metabolism on drugs and prodrugs in cases where metabolizing enzymes are induced

or inhibited.

9 Dr. Henry Zeidan

Objectives(Cont’d)

Describe distinguishing characteristics of agonists, partial agonists,

and antagonists.

Define the terms affinity, efficacy and selectivity in the context of drug-receptor interactions.

Distinguish reversible and irreversible inhibition based on analysis of graphs.

10 Dr. Henry Zeidan

Dr. Henry Zeidan 11

Pharmacologic Principles

Drug

• Any chemical that affects the processes of a living organism

Pharmacology

• The study or science of drugs

Dr. Henry Zeidan 12


• Pharmacokinetics

• Pharmacodynamics

• Pharmaceutics

• Pharmacotherapeutics

• Pharmacognosy

Dr. Henry Zeidan 13


Pharmacodynamics

• The study of what the drug does to the body:

– The mechanism of drug actions in living tissues

Dr. Henry Zeidan 14


Pharmaceutics

• The study of how various drug forms influence pharmacokinetic and pharmacodynamic activities

Dr. Henry Zeidan 15


Pharmacotherapeutics

• The use of drugs and the clinical indications for drugs to prevent and treat diseases

Dr. Henry Zeidan 16


Pharmacognosy

• The study of natural (plant and animal) drug sources

Pharmacokinetics vs. Pharmacodynamics(Con’d)

• Pharmacodynamics

• Action of the chemical on the body (“What the drug does to the body”)

• Process: Biological ligands acting on their molecular targets in the body.

• Output: Biological response

17 Dr. Henry Zeidan

Dr. Henry Zeidan 18


Pharmacokinetics

• The study of what the body does to the drug:

– Absorption

– Distribution

– Metabolism

– Excretion

Pharmacokinetics

19

Dr. Henry Zeidan

Schematic representation of absorption, distribution, metabolism and elimination

Lippinicott’s Illustrated Reviewes in Pharmacology, 2006

Pharmacokinetics (cont’d) Biotransformation and Elimination of Drugs(Cont’d)

• The major objective of drug biotransformation

reactions in the body is to make nonpolar

drugs more polar so that they may be more

readily excreted.

20 Dr. Henry Zeidan

Pharmacokinetics (cont’d) ADME (Absorption, Distribution, Metabolism,

Excretion)

• Majority of drugs exert their effects (pharmacodynamics) via interaction with specific receptor molecules within the body. However, prior to gaining access

to these targets the drug must:

• Pass thru barriers (membranes) • Avoid alternate sites of attachment and storage • Avoid metabolic destruction prior to reaching site of action • Be chemically stable at various pH levels • All 4 of these barriers will affect a drug’s pharmacokinetics.

21 Dr. Henry Zeidan

Pharmacokinetics (cont’d)

• When the drug reaches the desired site of action (enabling a pharmacodynamic response):

• Drug + Receptor Drug receptor complex

Pharmacological response

22 Dr. Henry Zeidan

Pharmacokinetics (cont’d) Biotransformation and Elimination of Drugs

• There are two primary ways in which drugs are eliminated from the body:

They may be excreted in the urine or feces (i.e., excreted unchanged); or

They may be metabolized or biotransformed and then excreted. (in some cases, drugs may be eliminated in other ways such as through respiration or through sweating, but these methods are decidedly in the minority).

23 Dr. Henry Zeidan


• Drugs are biotransformed prior to excretion primarily

because they are not polar enough to be excreted in the urine or feces. • The major objective of drug biotransformation reactions

in the body is to make nonpolar drugs more polar so that they may be more readily excreted.

24 Dr. Henry Zeidan


• Biotransformation results not only in making a drug more soluble for excretion, but also often produces a metabolite that is no longer capable of producing a therapeutic response. • In some cases, however, the drug itself is inactive and the process of biotransformation results in the active compound.

•

25 Dr. Henry Zeidan


26 Dr. Henry Zeidan


• Prodrugs • • A “Pro”drug is an inactive compound that is administered and then transformed into an active substance by either chemical or metabolic means • Prodrugs are designed to take advantage of

absorption or metabolic properties to provide more optimal drug therapy.

27 Dr. Henry Zeidan


• Prodrugs can be activated in various places

(e.g. stomach, intestine, liver, blood, inside

cells) and in various ways (cleavage of groups,

biotransformation, addition of phosphates)

28 Dr. Henry Zeidan


• In this case, the drug acts as a prodrug and

must be biotransformed in order to have a

therapeutic response.

29 Dr. Henry Zeidan

Biotransformation and Elimination of Drugs(Cont’d)

Prodrugs(Cont’d)

• Examples of Prodrugs

• Chloramphenicol succinate – esterified form

is more soluble and can be administered IV –

esterases in blood release active form (i.e.

chloramphenicol itself )

•

30 Dr. Henry Zeidan

31 Dr. Henry Zeidan

Examples of Prodrugs Chloramphenicol

succinate(Cont’d)

Biotransformation and Elimination of Drugs(Cont’d) Examples of Prodrugs (Cont’d)

• Sulindac – (A drug that have anti-inflammatory and

analgesic activity) in its active form (sulfide) causes significant GI irritation when administered orally . If the suldinac in its inactive form is absorbed from the GI tract and reduced by enzymes in the liver, the active form will be available only after absorption thus by passing the GI tract and reducing GI distress. •

32 Dr. Henry Zeidan

H

CH3

CH2COOH

F

S

O

OH3C

H

CH3

CH2COOH

F

S

CH3

O

H

CH3

CH2COOH

F

S

CH3

Sulfide (active) Sulindac (inactive) Sulfone (inactive)

Biotransformation and Elimination of Drugs(Cont’d) Examples of Prodrugs (Cont’d)

33 Dr. Henry Zeidan


34 Dr. Henry Zeidan Routes of drug administration

Lippincott’s Illustrated Reviewes in Pharmacology, 2008

Dr. Henry Zeidan 35 Reproduced from Lippicott’s, 2007


First-pass mechanism can occur with orally administered drugs

Pharmacokinetics (cont’d) Absorption of Drugs

36 Dr. Henry Zeidan

Schematic representation of drugs crossing a cell memebrane of an epithelial cell of

GI

Lippincott’s Illustrated Reviewes in Pharmacology, 2008

37

Lipid Bilayer

Small,

uncharged

Large,

uncharged

Small

charged

ions

H2O, urea,

CO2, O2, N2

Glucose

Sucrose

H+, Na+, K+,

Ca2+, Cl-,

HCO3-

X

Membranes and Absorption

X

X

Dr. Henry Zeidan

38 Dr. Henry Zeidan

Pharmacokinetics (cont’d)Absorption of

Drugs

A. Diffusion of the non-ionizrf for of a eak acid through a lipid membranep,

B. Diffusion of the non Ionized form of a weak base through a lipid membrane

Lipicott’s Illustrated Reviews in Pharmacology

Pharmacokinetics (cont’d) Distribution of Drugs

39 Dr. Henry Zeidan

The distribution of a drug between its ionized and non-ionized forms,

pKa value for the drug is 6.5

Lippincott’s Illustrated Reviews in Pharmacology

40

Factors Affecting Absorption

– Absorbing surface

– Blood flow

– pH

– Disease states

– Interactions with food, other drugs

– Drug pka

– Concentration

– Contact time at the absorption surface

Dr. Henry Zeidan Dr. Henry Zeidan


Factors Affecting Absorption(Cont’d)

How much drug will be found on either side of the membrane?

42 Dr. Henry Zeidan

43 Dr. Henry Zeidan

Pharmacokinetics (cont’d) Determination of Bioavailabilty of a drug

Lippincott’s Illustrated Reviews in Pharmacology

44

Distribution

• Rate of perfusion

• Plasma protein (albumin) binding

• Accumulation in tissues

• Ability to cross membranes

– Blood-brain barrier

– Placental barrier

Dr. Henry Zeidan

Dr. Henry Zeidan 45

Pharmacokinetics: Distribution

The transport of a drug in the body by the bloodstream to its site of action.

• Protein-binding

• Water soluble vs. fat soluble

• Blood-brain barrier

• Areas of rapid distribution: heart, liver, kidneys, brain

• Areas of slow distribution: muscle, skin, fat

Dr. Henry Zeidan 46

Pharmacokinetics: Bioavailability

• The rate at which a drug leaves its site of administration, and the extent to which absorption occurs.

– Bioavailability

– Bioequivalent

Pharmacokinetics (cont’d) Apparent volume of distribution

47 Dr. Henry Zeidan

Drug concentrations in serum after a single injection of drug at time =O,

Assume the drud is not eliminated Lippincott’s Illustrated Reviewes in Pharmacology


48 Dr. Henry Zeidan

Drug concentrations in serum after a single injection of drug at time =O.

Assume that the drugs distributes and is eliminiate

Dr. Henry Zeidan 49

Reproduced from Lippicott’s, 2007

Determination of Apparent volume of distribution

50 Dr. Henry Zeidan


Drug concentrations in serum after a single injection of drug at time =O.


Pharmacokinetics (cont’d) Binding Drugs to Plasma proteins

51 Dr. Henry Zeidan


Pharmacokinetics (cont’d) Binding Drugs to Plasma proteuns

52 Dr. Henry Zeidan

Binding of Class I and Class II drugs to serum albumin when drugs

are administered alone or together

Dr. Henry Zeidan 53

Drug Metabolism

Pharmacokinetics (cont’d) Effect of drug dose on the rate of Metabolism

54 Dr. Henry Zeidan

Dr. Henry Zeidan 55


Reactions of Drug Metabolism

Phase I

Phase I reactions function to convert lipophilic molecules into more

polar by introducing or unmasking polar functional group such as –OH,

or,-NH2

Phase I metabolism may increase, decrease, or leave unaltered

the drug’s pharmacologic action.

Phase II

This phase consists of conjugation reactions



The biotransformation of drugs

57

Metabolism (Biotransformation)

• Two effects

– Transformation of drugs to less, or more active metabolite

– Alteration of solubility

• Liver = primary site

• Liver disease

– Slows metabolism

– Prolongs effects

Dr. Henry Zeidan

Cytochrome P450 Monooxygenase System

• The cytochrome P450 enzymes are heme- containing membrane proteins that are capable of catalyzing the following types of reactions: • • Aromatic and aliphatic hydroxylations • N-, O-, and S- dealkylations • N-oxidation • Sulfoxidation • N-hydroxylation • Deamination

58 Dr. Henry Zeidan

Dr. Henry Zeidan 59



60 Dr. Henry Zeidan


61 Dr. Henry Zeidan

62

Elimination

• Kidneys = primary site

– Mechanisms dependent upon:

• Passive glomerular filtration

• Active tubular transport

– Partial reabsorption

– Hemodialysis

• Renal disease

– Slows excretion

– Prolongs effects

Dr. Henry Zeidan

Elimination(Cont’d)

63 Dr. Henry Zeidan

Dr. Henry Zeidan 64

Kinetics of Continous Administrtion


65 Dr. Henry Zeidan


66 Dr. Henry Zeidan

67

Biological Half-life (t 1/2)

• Amount of time to eliminate 1/2 of total drug

amount Shorter t 1/2 may need more frequent

doses.

• Hepatic disease may increase t1/2

Dr. Henry Zeidan


68 Dr. Henry Zeidan


69 Dr. Henry Zeidan


70 Dr. Henry Zeidan


71 Dr. Henry Zeidan

Dr. Henry Zeidan 72

Pharmacodynamics

73

Pharmacodynamics

• The biochemical and physiologic mechanisms of drug action

What the drug

does when it gets there?.

Dr. Henry Zeidan

74

Drug Mechanisms

• Receptor interactions

• Non-receptor mechanisms

Dr. Henry Zeidan

Dr. Henry Zeidan 75

Pharmacodynamics: Mechanisms of Action

• Receptor interaction

• Enzyme interaction

• Nonspecific interactions

76

Non-receptor Mechanisms

• Actions on Enzymes

– Enzymes = Biological catalysts

– Drugs alter processes catalyzed by the enzymes

– Examples

• Cholinesterase inhibitors

• Monoamine oxidase inhibitors

Dr. Henry Zeidan

77


• Combining With Other Chemicals

– Antacids

– Antiseptic effects of alcohol, phenol

- Chelation of heavy metals

. Changing Cell Membrane Permeability

Dr. Henry Zeidan

78


• Anti-metabolites

– Enter biochemical reactions in place of normal substrate “competitors”

– Result in biologically inactive product

– Examples

• Some anti-neoplastics

• Some anti-infectives

Dr. Henry Zeidan


Pharmacodynamics:

Dr. Henry Zeidan 80


Cumulative percent of patients responding to

plasma levels of drugs

Dr. Henry Zeidan 81

Dr. Henry Zeidan 82

Dr. Henry Zeidan 83

Dr. Henry Zeidan 84

Pharmacotherapeutics: Monitoring

• Therapeutic index

• Drug concentration

• Patient’s condition

• Tolerance and dependence

• Interactions

• Side effects/adverse drug effects

References:

• 1. Betram G. Katzung, Basic & Clinical Pharmacology, Ninth Edition, McGraw Hill

Richard A. Harvey, Pamela C. Champe,

• Lippincott’s Illustrated Reviews of Pharmacology, 4 edition,

85 Dr. Henry Zeidan

Dr. Henry Zeidan 86

END

usmle review series in pharmacology · 2012-09-22 · general principles in pharmacology objectives...

Documents